Matches in Nanopublications for { ?s ?p "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP207999.RAt05lWFIoj3mnv1j04kSZ8iSjkKjQDJ7OGZ6R7qTMlcY130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207999.RAt05lWFIoj3mnv1j04kSZ8iSjkKjQDJ7OGZ6R7qTMlcY130_provenance.
- NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312839.RAY2AxUaY7ulH3fk0UF7rRketwP09wPkWCnQ4_R5qjvOg130_provenance.
- NP899680.RA5stkboik1HuL7uWUToogtfJvzS-tFr_tvmkw_j7UIg0130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899680.RA5stkboik1HuL7uWUToogtfJvzS-tFr_tvmkw_j7UIg0130_provenance.
- NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_provenance.
- NP1104769.RAB7y6gvZBNvzBRvUga5J9-58GNv__N1fJ714kGY47G3I130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1104769.RAB7y6gvZBNvzBRvUga5J9-58GNv__N1fJ714kGY47G3I130_provenance.